| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001272003.1 | 4055 | Intron | NP_001258932.1 | ||
| NM_020822.2 | 4055 | Intron | NP_065873.2 | ||
| XM_011518877.2 | 4055 | Missense Mutation | CAC,CGC | H49R | XP_011517179.1 |
| XM_011518878.2 | 4055 | Missense Mutation | CAC,CGC | H49R | XP_011517180.1 |
| XM_011518879.2 | 4055 | Missense Mutation | CAC,CGC | H49R | XP_011517181.1 |
| XM_011518880.1 | 4055 | Intron | XP_011517182.1 | ||
| XM_011518881.2 | 4055 | Intron | XP_011517183.1 | ||
| XM_017014931.1 | 4055 | Intron | XP_016870420.1 | ||
| XM_017014932.1 | 4055 | Intron | XP_016870421.1 | ||
| XM_017014933.1 | 4055 | Intron | XP_016870422.1 |